Canonical Allele Identifier: CA377326147

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739997G>T (hg19) ; chr10:g.77980239G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980239G>T , CM000672.2:g.77980239G>T	GRCh38
NC_000010.10:g.79739997G>T , CM000672.1:g.79739997G>T	GRCh37
NC_000010.9:g.79410003G>T	NCBI36
NG_029648.1:g.54302C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1843C>A
ENST00000698725.1:n.1596C>A
ENST00000698726.1:n.3156C>A
ENST00000698727.1:n.2889C>A
ENST00000698728.1:n.3505C>A
ENST00000698729.1:n.4953C>A
ENST00000698730.1:n.5051C>A
ENST00000698731.1:c.3785C>A	ENSP00000513898.1:p.Ala1262Asp
ENST00000698732.1:c.*2615C>A	ENSP00000513899.1:n.*2615C>A
ENST00000698733.1:c.*3113C>A	ENSP00000513900.1:n.*3113C>A
ENST00000698734.1:c.*2099C>A	ENSP00000513901.1:n.*2099C>A
ENST00000698735.1:n.4277C>A
ENST00000698736.1:n.4690C>A
ENST00000698737.1:n.4041C>A
ENST00000372371.8:c.3926C>A MANE Select	ENSP00000361446.3:p.Ala1309Asp
ENST00000372371.7:c.3926C>A	ENSP00000361446.3:p.Ala1309Asp
ENST00000616246.4:c.374C>A	ENSP00000483738.1:p.Ala125Asp
NM_007055.3:c.3926C>A	NP_008986.2:p.Ala1309Asp
NM_007055.4:c.3926C>A MANE Select	NP_008986.2:p.Ala1309Asp